EP3710790A1 - Sensoranordnung und verfahren zur verwendung davon - Google Patents

Sensoranordnung und verfahren zur verwendung davon

Info

Publication number
EP3710790A1
EP3710790A1 EP18879086.9A EP18879086A EP3710790A1 EP 3710790 A1 EP3710790 A1 EP 3710790A1 EP 18879086 A EP18879086 A EP 18879086A EP 3710790 A1 EP3710790 A1 EP 3710790A1
Authority
EP
European Patent Office
Prior art keywords
sensor
base layer
substrate
electrode
fluid flow
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
EP18879086.9A
Other languages
English (en)
French (fr)
Other versions
EP3710790A4 (de
Inventor
Jennifer Samproni
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Siemens Healthcare Diagnostics Inc
Original Assignee
Siemens Healthcare Diagnostics Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Siemens Healthcare Diagnostics Inc filed Critical Siemens Healthcare Diagnostics Inc
Publication of EP3710790A1 publication Critical patent/EP3710790A1/de
Publication of EP3710790A4 publication Critical patent/EP3710790A4/de
Pending legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/26Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
    • G01N27/27Association of two or more measuring systems or cells, each measuring a different parameter, where the measurement results may be either used independently, the systems or cells being physically associated, or combined to produce a value for a further parameter
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/26Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
    • G01N27/28Electrolytic cell components
    • G01N27/30Electrodes, e.g. test electrodes; Half-cells
    • G01N27/327Biochemical electrodes, e.g. electrical or mechanical details for in vitro measurements
    • G01N27/3271Amperometric enzyme electrodes for analytes in body fluids, e.g. glucose in blood
    • G01N27/3272Test elements therefor, i.e. disposable laminated substrates with electrodes, reagent and channels
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/17Systems in which incident light is modified in accordance with the properties of the material investigated
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/483Physical analysis of biological material
    • G01N33/487Physical analysis of biological material of liquid biological material
    • G01N33/49Blood
    • G01N33/492Determining multiple analytes
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/543Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals
    • G01N33/54366Apparatus specially adapted for solid-phase testing
    • G01N33/54373Apparatus specially adapted for solid-phase testing involving physiochemical end-point determination, e.g. wave-guides, FETS, gratings
    • G01N33/5438Electrodes
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/17Systems in which incident light is modified in accordance with the properties of the material investigated
    • G01N2021/1734Sequential different kinds of measurements; Combining two or more methods

Definitions

  • the present disclosure relates to a sensing device which allows for multiple tests to be run concurrently using a small sample volume.
  • the present disclosure describes a method in which a sample is passed through a fluid flow path of a sensor assembly such that the sample intersects at least one sensor comprising at least three electrodes arranged such that two or more electrodes are opposing and two or more electrodes are beside one another.
  • the sensor is read by a reader monitoring changes to the sensor in the presence of the sample.
  • the reader measures the presence and/or concentration of one or more analytes within the sample based upon data obtained by the reader.
  • the present disclosure describes a sensor assembly provided with a first substrate, and a second substrate.
  • the first substrate comprises a first base layer, and a first electrical contact, the first base layer having a first surface and a second surface, a first sensor portion on the first surface and connected to the first electrical contact.
  • the second substrate comprises a second base layer, a second sensor portion, and a plurality of second electrical contacts, the second base layer having a first surface and a second surface with the second sensor portion on the first surface of the second base layer.
  • the first substrate and the second substrate are arranged in a layered structure in which the first surface of the first base layer and the first surface of the second base layer border a fluid flow path intersecting the first sensor portion and the second sensor portion, the first sensor portion aligned with the second sensor portion across the fluid flow path to form an electrochemical type of sensor.
  • the second sensor portion includes a first electrode and a second electrode with the first electrode electrically isolated from the second electrode.
  • the present disclosure describes a sensor assembly provided with a first substrate and a second substrate.
  • the first substrate comprises a first base layer, the first base layer having a first surface and a second surface, two spaced apart first sensor portions on the first surface.
  • the second substrate comprises a second base layer, the second base layer having a first surface and a second surface, two spaced apart second sensor portions on the first surface.
  • the first substrate and the second substrate are arranged in a layered structure in which the first surface of the first base layer and the first surface of the second base layer border a fluid flow path, one of the first sensor portions is aligned with one of the the second sensor portions across the fluid flow path to form a first sensor, and the other one of the first sensor portions is aligned with the other one of the second sensor portions across the fluid flow path to form a second sensor.
  • Each of the second sensor portions includes a first recognition element and a second recognition element.
  • the first recognition element and the second recognition element are electrodes.
  • Figure 1 is a top plan view of one embodiment of an exemplary sensor assembly constructed in accordance with the present disclosure.
  • Figure 2 is a cross-sectional diagram of the sensor assembly of Figure 1, taken along the lines 2—2.
  • Figure 3 is a cross-sectional diagram of the sensor assembly of Figure 1, taken along the lines 3—3.
  • Figure 4 is a diagrammatic, top plan view of a first substrate and a second substrate utilized to form the sensor assembly depicted in Figure 1.
  • Figure 5 is a block diagram illustrating a method of using the sensor assembly in accordance with the present disclosure.
  • Figures 6A and 6B are diagrammatic views of incorporating the sensor assembly into a fluidic housing in accordance with the present disclosure. DESCRIPTION OF THE PREFERRED EMBODIMENTS
  • inventive concepts are not limited in their application to the details of construction and the arrangement of the components or steps or methodologies set forth in the following description or illustrated in the drawings.
  • inventive concepts disclosed herein are capable of other embodiments or of being practiced or carried out in various ways.
  • phraseology and terminology employed herein is for the purpose of description and should not be regarded as limiting the inventive concepts disclosed and claimed herein in any way.
  • compositions comprising, “comprising,” “includes,” “including,” “has,” “having” or any other variation thereof, are intended to cover a non-exclusive inclusion.
  • a composition, a process, method, article, or apparatus that comprises a list of elements is not necessarily limited to only those elements but may include other elements not expressly listed or inherently present therein.
  • the terms “approximately,” “about,” “substantially” and variations thereof are intended to include not only the exact value qualified by the term, but to also include some slight deviations therefrom, such as deviations caused by measuring error, manufacturing tolerances, wear and tear on components or structures, settling or precipitation of cells or particles out of suspension or solution, chemical or biological degradation of solutions over time, stress exerted on structures, and combinations thereof, for example.
  • sample and variations thereof is intended to include biological tissues, biological fluids, chemical fluids, chemical substances, suspensions, solutions, slurries, mixtures, agglomerations, tinctures, slides, powders, or other preparations of biological tissues or fluids, synthetic analogs to biological tissues or fluids, bacterial cells (prokaryotic or eukaryotic ), viruses, singlecelled organisms, lysed biological cells, fixed biological cells, fixed biological tissues, cell cultures, tissue cultures, genetically engineered cells and tissues, genetically engineered organisms, and combinations thereof, for example.
  • the sample can be in a liquid or a gaseous form.
  • any reference to "one embodiment” or “an embodiment” means that a particular element, feature, structure, or characteristic described in connection with the embodiment is included in at least one embodiment.
  • the appearances of the phrase “in one embodiment” in various places in the specification are not necessarily all referring to the same embodiment.
  • the inventive concepts disclosed herein are generally directed to the need to minimize the sample volume required to test two or more analytes concurrently.
  • Low sample volumes are desirable when the sample is limited, such as in the case of neonatal patients, or when the sample itself is expensive.
  • the required sample volume can be greatly reduced when recognition elements of the sensors are arranged in a combination in which two or more recognition elements are facing one another in a sandwich configuration (also referred to as an opposing sensor array) and two or more recognition elements are in a non-opposing configuration which is also referred to herein as a side-by- side configuration or a coplanar configuration.
  • a sandwich configuration also referred to as an opposing sensor array
  • two or more recognition elements are in a non-opposing configuration which is also referred to herein as a side-by- side configuration or a coplanar configuration.
  • Illustrative opposing and co-planar sensor arrays are discussed in connection with Figures 1-4 below.
  • FIG. 10 shown therein and designated by reference numeral 10 is one embodiment of a sensor assembly constructed in accordance with the present disclosure.
  • Figure 2 is a cross-sectional view of the sensor assembly 10 taken along the lines 2-2
  • Figure 3 is another cross-sectional diagram of the sensor assembly 10 taken along the lines 3—3 depicted in Figure 1.
  • the sensor assembly 10 includes a plurality of sensors 11 positioned within a housing 12.
  • three sensors 11 are shown and designated by reference numerals l la, l lb and l lc by way of example. It should be understood that the sensor assembly 10 may be provided with more or less of the sensors 11.
  • the sensors 11 can be configured to identify the same analyte of interest or different analytes of interest.
  • the sensor l la can be configured to detect an electrolyte
  • the sensor 1 lb can be configured to detect glucose
  • the sensor l lc can be configured to detect neonatal total bilirubin (nBili).
  • the sensor assembly 10 is provided with a first substrate 14, and a second substrate 18, which collectively form the housing 12.
  • the first substrate 14 and the second substrate 18 are shaped so as to form a fluid flow path 20 in which the sensors l la-c are disposed.
  • the sensors 11 are formed of multiple electrodes that are spaced apart and electrically isolated from one another.
  • the sensors 11 may be used to identify and/or measure analytes of interest in the analysis of clinical chemicals such as blood gases, electrolytes, metabolites, DNA and antibodies, including basic and applied research.
  • Each of the sensors 11 is capable of providing specific quantitative or semi-quantitative analytical information using a biological recognition element (biochemical receptor).
  • the sensors 11 may be classified according to the biological specificity-conferring mechanism or, alternatively, the mode of physicochemical signal transduction.
  • the biological recognition element may be based on a chemical reaction catalysed by, or on an equilibrium reaction with, macromolecules that have been isolated, engineered or present in their original biological environment. In the latter case, equilibrium is generally reached and there is no further, if any, net consumption of analyte(s) by the immobilized biocomplexing agent incorporated into the sensor 11.
  • the sensors 11 may be further classified according to the analytes or reactions that they monitor: direct monitoring of analyte concentration or of reactions producing or consuming such analytes; alternatively, an indirect monitoring of inhibitor or activator of the biological recognition element (biochemical receptor) may be achieved.
  • the sensors 11 may be of various types.
  • the sensors 11 may be selected from the group comprising an electrochemical sensor, an amperometric sensor, a blood glucose sensor, a potentiometric sensor, a conduct metric sensor, a thermometric sensor, an optical sensor, a fiber optic lactate sensor, a piezoelectric sensor, an immuno- sensor or the like.
  • the sensors 11 may be disposable after one measurement, i.e., single use, and unable to monitor and analyte concentration continuously or at multiple instances of time.
  • the sensors 11 may be multi-use in which the sensors 11 are adapted to monitor an analyte concentration continuously or at multiple instances of time.
  • the sensors 11 described herein are integrated devices utilized for detecting analytes of interest, and can be distinguished from an analytical system which incorporates additional separation steps such as high-performance liquid chromatography, or additional hardware and/or sample processing such as specific reagent introduction to identify an analyte of interest.
  • the sensors 11 are reagentless analytical devices.
  • the sensors 11 will be described herein by way of example as an electrochemical type of sensor. It should be understood, however, that the skilled artisan will understand how to create other types of sensors 11 based upon the teachings within the present disclosure.
  • the electrochemical type of sensor 11 is capable of providing specific quantitative or semi-quantitative analytical information using a biological recognition element (biochemical receptor) which is retained in direct spatial contact with an electrochemical transduction element.
  • the electrochemical type of sensor 11 may be based upon the principle of a transfer of charge from an electrode to another electrode based upon an oxidation or reduction process. During this process, chemical changes take place at the electrodes and the charge is conducted through the sample. By measuring the transfer of charge, a determination of the presence and/or the amounts of analytes of interest may be made.
  • Electrochemical types of sensors 11 may be based upon several principles, such as potentiometric, amperometric, or conductivity measurements. Also, the electrochemical type of sensors 11 may have the ability to be repeatedly calibrated without any reagent addition.
  • the electrochemical type of sensor 11 is provided with at least three recognition elements in the form of electrodes, that may be classified as a working electrode, a counter electrode, and a reference electrode.
  • a voltage potential difference between certain of the electrodes (e.g., a working electrode and a counter electrode) forming the electrochemical type of sensor 11 is read and interpreted.
  • a current that is dependent upon the concentration of an analyte is read and interpreted. In some instances, the amount of the current is linearly dependent upon the concentration of analyte.
  • Conductometric sensors are based on the measurement of electrolyte conductivity, which varies when the sensor is exposed to different environments.
  • the electrodes of the electrochemical type of sensor 11, in general, are fabricated of predetermined materials, dopings and/or coatings to provide analyte selectivity to the electrochemical type of sensor 11.
  • the biological receptors i.e.
  • enzymes, antibodies, cells or tissues, with high biological activity can be immobilized in a thin layer at the transducer surface by using different procedures, such as entrapment behind a membrane, entrapment within a polymeric matrix, entrapment of biological receptors within self-assembled monolayers or bilayer lipid membranes, covalent bonding of receptors on membranes or surfaces activated by bifunctional groups of spacers, or bulk modification of entire electrode material.
  • Receptors may be immobilized either alone or may be mixed with other proteins, such as bovine serum albumin (BSA), either directly on the electrode, or on a polymer membrane covering the electrode. In the latter case, preactivated membranes can be used directly for the enzyme or antibody immobilization without further chemical modification of the membrane or macromolecule.
  • BSA bovine serum albumin
  • the first substrate 14 is provided with a first base layer 22, and a plurality of first electrical contacts 26 (three of the first electrical contacts 26 being depicted in Figure 2 by way of example and designated by reference numerals 26a, 26b, and 26c).
  • the first base layer 22 may be made from, for example, ceramic, polymer, foil, or any other type of material known to someone of ordinary skill in the art.
  • the first electrical contacts 26 are electrically isolated and may be constructed of an electrically conductive material, such as copper, aluminum, silver, gold, carbon nanotubes, or the like.
  • the first base layer 22 may be provided with a first surface 30, and a second surface 32.
  • the first surface 30 may be a planar surface, i.e., in the form of a plane. In other embodiments, the first surface 30 may be in the form of an arc, or include a combination of planar and arc shaped portions.
  • the first electrical contacts 26 may extend through the first base layer 22 from the first surface 30 to the second surface 32 as shown in Figure 2 so that a reader (not shown) can be connected to the first electrical contacts 26. In other embodiments, the first electrical contacts 26 may extend across portions of the first surface 30 and/or the second surface 32 so long as the first electrical contacts 26 may be connected to a reader.
  • the first substrate 14 is also provided with a plurality of first sensor portions 36 connected to and on the first surface 30.
  • the first sensor portions 36 extend over and cover at least a portion of the first surface 30.
  • the first sensor portions 36 do not directly contact the first surface 30. Rather, one or more layers of material may be positioned between the first sensor portions 36 and the first surface 30.
  • the first surface 30 is devoid of any reaction wells or other areas designed to retain a liquid around the first sensor portions 36.
  • each of the first sensor portions 36 forms a part of one of the electrochemical sensors 11.
  • three of the first sensor portions 36 are depicted and labeled with reference numerals 36a, 36b and 36c.
  • the first sensor portions 36 are spaced apart and electrically isolated from one another. Although the first sensor portions 36 are shown spaced apart in a generally linear arrangement, it should be understood that other arrangements and patterns of the first sensor portions 36 can be used in an effort to maximize the density of the first sensor portions 36. For example, the first sensor portions 36 can be arranged in a staggered arrangement. In the example depicted in Figures 2 and 4, the first sensor portion 36a is spaced apart from the first sensor portion 36b and electrically isolated therefrom. Likewise, the first sensor portion 36b is spaced apart from the first sensor portion 36c and electrically isolated therefrom. Although only three of the first sensor portions 36 are depicted, it should be understood that the first substrate 14 can be provided with more or less of the first sensor portions 36.
  • the first sensor portions 36 can be made of an electrically conductive material using any suitable methodology, such as a thick film approach (e.g., screen printing, rotogravure, pad printing, stenciling conductive material such as carbon, Cu, Pt, Pd, Au, and/or Nanotubes, etc ) or a thin film approach (e.g., by spuhering, thermal spraying, and/or cold spraying conductive material). While the first sensor portions 36 in Figure 4 are depicted as being rectangular, it should be understood that this is an exemplary configuration only. The first sensor portions 36 could be constructed in various shapes, such as a line, a circle, a triangle or the like.
  • Respective ones of the first electrical contacts 26 are connected to the first sensor portions 36.
  • the first electrical contact 26a is connected to the first sensor portion 36a; the first electrical contact 26b is connected to the first sensor portion 36b; and the first electrical contact 26c is connected to the first sensor portion 36c.
  • the second substrate 18 is provided with a second base layer 50, and a plurality of second electrical contacts 52 (six of the second electrical contacts 52 being depicted in Figure 2 by way of example and designated by reference numerals 52a, 52b, 52c, 52d, 52e and 52f).
  • the second base layer 50 may be made from, for example, ceramic, polymer, foil, or any other type of material known to someone of ordinary skill in the art.
  • the second electrical contacts 52 are electrically isolated and may be constructed of an electrically conductive material, such as copper, aluminum, silver, gold, carbon nanotubes, or the like. It should be understood that in some embodiments the first electrical contacts 26 and the second electrical contacts 52 are optional.
  • the first electrical contacts 26 and the second electrical contacts 52 may not be included when the sensor 11 is an optical type of sensor that can be read by an optical reader, such as a reflectance meter or a photodetector.
  • the second base layer 50 may be provided with a first surface 56, and a second surface 60.
  • the second electrical contacts 52 may extend through the second base layer 22 from the first surface 56 to the second surface 60 as shown in Figure 2 so that a reader (not shown) can be connected to the second electrical contacts 26.
  • the second electrical contacts 52 may extend across portions of the first surface 56 and/or the second surface 60 so long as the second electrical contacts 52 may be connected to a reader.
  • the second substrate 18 is also provided with a plurality of second sensor portions 64 on the first surface 56.
  • the second sensor portions 64 extend over and cover at least a portion of the first surface 56.
  • the second sensor portions 56 do not directly contact the first surface 56. Rather, one or more layers of material may be positioned between the second sensor portions 36 and the first surface 56.
  • the first surface 56 is devoid of any reaction wells or other areas designed to retain a liquid around the second sensor portions 64.
  • the first surface 36 can be shaped to form one or more reaction wells encompassing respective ones of the second sensor portions.
  • a combination of the first and second sensor portions 64 forms one of the electrochemical sensors 11.
  • the second sensor portions 64 are depicted and labeled with reference numerals 64a, 64b and 64c.
  • the second sensor portions 64 are spaced apart and electrically isolated from one another.
  • the second sensor portions 64 are shown spaced apart in a generally linear arrangement, it should be understood that other arrangements and pahems of the second sensor portions 64 can be used in an effort to maximize the density of the second sensor portions 64 on the first surface 56.
  • the second sensor portions 64 can be arranged in a staggered arrangement.
  • the second sensor portion 64a is spaced apart from the second sensor portion 64b and electrically isolated therefrom.
  • the second sensor portion 64b is spaced apart from the second sensor portion 64c and electrically isolated therefrom.
  • the second sensor portions 64 can be made of an electrically conductive material using any suitable methodology, such as a thick film approach (e.g., screen printing, rotogravure, pad printing, stenciling conductive material such as carbon, Cu, Pt, Pd, Au, and/or Nanotubes, etc ... ) or a thin film approach (e.g., by sputtering, thermal spraying, and/or cold spraying conductive material).
  • a thick film approach e.g., screen printing, rotogravure, pad printing, stenciling conductive material such as carbon, Cu, Pt, Pd, Au, and/or Nanotubes, etc ...
  • a thin film approach e.g., by sputtering, thermal spraying, and/or cold spraying conductive material.
  • the first substrate 14 and the second substrate 18 are arranged in a layered structure in which the first surface 30 of the first base layer 22 extends over and covers the first surface 56 of the second base layer 50.
  • the first surface 30 of the first base layer 22 and the first surface 56 of the second base layer 50 also border the fluid flow path 20.
  • the first substrate 14 can be bonded to the second substrate 18 in a variety of manners, such as using a cohesive, an adhesive, pressure sensitive adhesive, ultraviolet adhesive, thermal adhesive, ultrasonic welding, thermal tacking procedures, or mechanical coupling (e.g., tongue and groove construction).
  • the first sensor portions 36 are aligned with the second sensor portions 64 and spaced apart there from so that the sample can flow between the first sensor portions 36 and the second sensor portion 64.
  • the first sensor portion 36 can be characterized as a single electrode 70.
  • the first sensor portion 36 and the second sensor portion 64 of each electrochemical type of sensor 11 is spaced apart vertically an amount sufficient to electrically isolate the first sensor portion 36 from the second sensor portion 64 in the absence of a sample contacting the first sensor portion 36 and the second sensor portion 64, while permitting the first sensor portion 36 and the second sensor portion 64 to work together to identify an analyte of interest in the presence of the sample.
  • the electrochemical type of sensors 11 are spaced laterally from one another the amount of spacing can be determined based upon the types of sensors 11, the types of samples anticipated to be analyzed, and a desired useful life of the sensor. For example, when the sensors 11 will be used for identifying analytes of interest in blood, and have a desired useful life of 30 days, then a lmm spacing between sensors 11 can be used. If a shorter useful life is desired, then the sensors 11 can be spaced closer together.
  • the second sensor portions 64 are provided with two or more electrodes.
  • the second sensor portions 64 include a first electrode 72 and a second electrode 74 with the first electrode 72 electrically isolated from the second electrode 74 in the absence of a sample contacting the first electrode 72 and the second electrode 74.
  • the first electrode 72 and the second electrode 74 are spaced apart a sufficient distance to maintain electrical isolation in the absence of a sample contacting the first electrode 72 and the second electrode 74, while establishing fluidic contact in the presence of the sample to permit the first and second electrodes 72 and 74 to work together to assist in identifying the analyte of interest.
  • each of the electrochemical type of sensors 11 include a single electrode 70 residing on the first surface 30 of the first base layer 22, and the first electrode 72, and the second electrode 74 residing on the first surface 56 of the second base layer 50.
  • first and second electrodes 72 and 74 in Figure 4 are depicted as being rectangular, it should be understood that this is an exemplary configuration only.
  • the first and second electrodes 72 and 74 of the second sensor portions 64 could be constructed in various shapes, such as a line, a circle, an arc shape, a triangle or the like.
  • the first surface 56 of the second base layer 50 is a planar surface.
  • the first and second electrodes 72 and 74 are arranged in a co-planar configuration.
  • the electrodes 70, 72 and 74 of the electrochemical type of sensors 11 are arranged in a combination in which two or more electrodes (e.g., the electrodes 70 and 74) are connected to different support structures (in this case the electrode 70 is connected to the first substrate 14 and the electrode 74 is connected to the second substrate 18) and face one another in a sandwich configuration (also referred to as an opposing sensor array) across the fluid flow path 20, and two or more electrodes (e.g., the electrodes 72 and 74) are connected to a same surface of a support structure (in this example the first surface 56 of the second substrate 18) in a coplanar configuration.
  • two or more electrodes e.g., the electrodes 70 and 74
  • the electrodes 72 and 74 are connected to a same surface of a support structure (in this example the first surface 56 of the second substrate 18) in a coplanar configuration.
  • the electrode 70 can be a reference electrode
  • the electrode 72 can be a working electrode
  • the electrode 74 can be a counter electrode.
  • one or more of the electrochemical sensors 11 could also have an inactive working electrode. In this instance, the inactive working electrode would be a part of the second sensor portion 64.
  • Respective ones of the second electrical contacts 52 are connected to the second sensor portions 64.
  • the second electrical contact 52a is connected to the electrode 72 of the electrochemical type of sensor l la
  • the second electrical contact 52b is connected to the electrode 74 of of the electrochemical type of sensor l la
  • the second electrical contact 52c is connected to the electrode 72 of the electrochemical type of sensor l la
  • the second electrical contact 52d is connected to the electrode 74 of the electrochemical type of sensor l lb
  • the second electrical contact 52e is connected to the electrode 72 of the electrochemical type of sensor l lc
  • the second electrical contact 52f is connected to the electrode 74 of the electrochemical type of sensor 1 lc.
  • the second substrate 18 may also be provided with two spaced apart side walls 80, 82, and end walls 83, 84 extending between the first surface 30 of the first base layer 22 and the first surface 56 of the second base layer 50 to define the fluid flow path 20.
  • the first surface 30 of the first base layer 22, the first surface 56 of the second base layer 50, the sidewalls 80, 82, and the end walls 83, 84 border the fluid flow path 20.
  • the sidewalls 80, 82, and the end walls 83, 84 may be integrally formed with the second base layer 50 to form a unitary structure.
  • the sidewalls 80, 82, and end walls 83, 84 may be applied onto the first surface 30 of the first base layer 22, or the first surface 56 of the second base layer 50.
  • the sidewalls 80, 82, and end walls 83, 84 are designed so as to not interfere with the reactions (e.g., electrochemical reactions) caused by an interaction with the sample and the electrochemical type of sensors 11.
  • the sidewalls 80, 82, and end walls 83, 84 are either constructed with a dielectric material, or coated with a dielectric material. It should also be understood that the sidewalls 80, 82, and end walls 83, 84 may be integral with or bonded to the first base layer 22.
  • the sidewalls 80, 82, and end walls 83, 84 may be referred to herein as a dielectric layer having an opening 85 (see Figure 4) forming the fluid flow path 20 and being closed by the first base layer 22 or the second base layer 50.
  • the sensor assembly 10 is also provided with a first end 86 and a second end 88.
  • the fluid flow path 20 extends generally between the first end 86 and the second end 88, but is separate from (i.e., does not intersect) either one of the first end 86 or the second end 88.
  • the first base layer 22 may be provided with an inlet 90 and an outlet 92 that intersect the fluid flow path 20 when the first substrate 14 is bonded to the second substrate 18.
  • the inlet 90 and the outlet 92 extend through the first base layer 22 from the first surface 30 to the second surface 32 to permit a sample to be disposed within the fluid flow path 20 and flow from the inlet 90 to the outlet 92.
  • inlet 90 and/or outlet 92 may be formed in a variety of ways.
  • inlet 90 and/or outlet 92 may be openings in the side of the sensor assembly 10, may be ports (e.g., apertures) formed in one or more layers of first and second substrates 14 and 18.
  • the first and second substrates 14 and 18 can be designed for the fluid flow path 20 to intersect either one or both of the first end 86 or the second end 88.
  • the first and second substrates 14 and 18 can be designed to provide two or more fluid flow paths 20, e.g., with one or more of the electrochemical sensors 11 in one or more of the fluid flow paths 20.
  • Figure 5 shows a process 100 of measuring the presence and/or concentration of an analyte in accordance with the presently disclosed concepts.
  • the sample is passed through the fluid flow path 20 as indicated by a block 102. This can be accomplished by introducing the sample into the fluid flow path 20 and using a motive force, such as a pump or capilarry action, to move the sample through the fluid flow path 20 to intersect the sensors 11 a, l lb or l lc as shown in block 104.
  • a motive force such as a pump or capilarry action
  • the first electrical contacts 26 and the second electrical contacts 52 can be read by a reader when certain ones of the sensors 11 are of the electrochemical type.
  • light emitted from the sensors 11 that are of an optical type e.g., fluoresce in the presence of an analyte of interest
  • an optical detector such as a photodetector or a grid of photodetectors.
  • the reader(s) receive the information (e.g., changes in voltage, amperage, or conductivity, optical signals, or the like), and uses the information to measure the presence and/or concentration of one or more analytes within the sample as indicated by block 108.
  • Figures 6A and 6B depict an embodiment in which sensor assembly 10 is incorporated into a fluidic housing 110.
  • Fluidic housing 110 may be made of molded plastic and/or polymer and have microfluidic and/or macrofluidic channels 112 incorporated therein (represented by the dashed arrows/box).
  • the sensor assembly 10 can then be inserted into an opening 114 into the housing 110 such that the fluid flow path(s) 20 are placed in fluidic contact with the microfluidic and/or macrofluidic channels 112 such that liquid flows through from the channels 112 into the sensor assembly 10 and back into the channels 112 in the direction of the fluid flow path 20.
  • Sensor assembly 10 can be bonded to the fluidic housing 110 via, for example, adhesive, ultrasonic welding, thermal sealing, and solvent bonding, etc.
  • the present disclosure describes a method in which a sample is passed through a fluid flow path of a sensor assembly such that the sample intersects at least one sensor comprising at least three electrodes arranged such that two or more electrodes are opposing and two or more electrodes are beside one another.
  • the sensor is read by a reader monitoring changes to the sensor.
  • the reader measures the presence and/or concentration of one or more analytes within the sample based upon data obtained by the reader.
  • the present disclosure describes a sensor assembly provided with a first substrate, and a second substrate.
  • the first substrate comprises a first base layer, and a first electrical contact, the first base layer having a first surface and a second surface, a first sensor portion on the first surface and connected to the first electrical contact.
  • the second substrate comprises a second base layer, a second sensor portion, and a plurality of second electrical contacts, the second base layer having a first surface and a second surface with the second sensor portion on the first surface of the second base layer.
  • the first substrate and the second substrate are arranged in a layered structure in which the first surface of the first base layer and the first surface of the second base layer border a fluid flow path intersecting the first sensor portion and the second sensor portion, the first sensor portion aligned with the second sensor portion across the fluid flow path to form an electrochemical type of sensor.
  • the second sensor portion includes a first electrode and a second electrode with the first electrode electrically isolated from the second electrode.
  • the present disclosure describes a sensor assembly provided with a first substrate and a second substrate.
  • the first substrate comprises a first base layer, the first base layer having a first surface and a second surface, two spaced apart first sensor portions on the first surface.
  • the second substrate comprises a second base layer, the second base layer having a first surface and a second surface, two spaced apart second sensor portions on the first surface.
  • the first substrate and the second substrate are arranged in a layered structure in which the first surface of the first base layer and the first surface of the second base layer border a fluid flow path, one of the first sensor portions is aligned with one of the the second sensor portions across the fluid flow path to form a first sensor, and the other one of the first sensor portions is aligned with the other one of the second sensor portions across the fluid flow path to form a second sensor.
  • Each of the second sensor portions includes a first recognition element and a second recognition element.
  • the first recognition element and the second recognition element are electrodes.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Immunology (AREA)
  • Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Pathology (AREA)
  • General Physics & Mathematics (AREA)
  • General Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Analytical Chemistry (AREA)
  • Molecular Biology (AREA)
  • Hematology (AREA)
  • Biomedical Technology (AREA)
  • Urology & Nephrology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Food Science & Technology (AREA)
  • Medicinal Chemistry (AREA)
  • Biophysics (AREA)
  • Microbiology (AREA)
  • Biotechnology (AREA)
  • Ecology (AREA)
  • Cell Biology (AREA)
  • Investigating Or Analyzing Materials By The Use Of Electric Means (AREA)
  • Optical Measuring Cells (AREA)
  • Apparatus Associated With Microorganisms And Enzymes (AREA)
  • Investigating Or Analysing Materials By Optical Means (AREA)
EP18879086.9A 2017-11-17 2018-11-16 Sensoranordnung und verfahren zur verwendung davon Pending EP3710790A4 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201762587856P 2017-11-17 2017-11-17
PCT/US2018/061556 WO2019099855A1 (en) 2017-11-17 2018-11-16 Sensor assembly and method of using same

Publications (2)

Publication Number Publication Date
EP3710790A1 true EP3710790A1 (de) 2020-09-23
EP3710790A4 EP3710790A4 (de) 2021-01-20

Family

ID=66539169

Family Applications (1)

Application Number Title Priority Date Filing Date
EP18879086.9A Pending EP3710790A4 (de) 2017-11-17 2018-11-16 Sensoranordnung und verfahren zur verwendung davon

Country Status (8)

Country Link
US (1) US12072311B2 (de)
EP (1) EP3710790A4 (de)
JP (2) JP2021503597A (de)
CN (1) CN111316072B (de)
CA (1) CA3082898C (de)
IL (1) IL274468A (de)
MX (1) MX2020005123A (de)
WO (1) WO2019099855A1 (de)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111316072B (zh) * 2017-11-17 2021-12-07 美国西门子医学诊断股份有限公司 传感器组件和使用所述传感器组件的方法
US20240260902A1 (en) * 2023-02-02 2024-08-08 Nerv Technology Inc. Modular sensor platform for inline biomarker monitoring

Family Cites Families (65)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6224141A (ja) 1985-07-25 1987-02-02 Matsushita Electric Works Ltd 化学物質検出器
US4911794A (en) * 1986-06-20 1990-03-27 Molecular Devices Corporation Measuring with zero volume cell
US5063081A (en) * 1988-11-14 1991-11-05 I-Stat Corporation Method of manufacturing a plurality of uniform microfabricated sensing devices having an immobilized ligand receptor
US6306594B1 (en) * 1988-11-14 2001-10-23 I-Stat Corporation Methods for microdispensing patterened layers
US5212050A (en) * 1988-11-14 1993-05-18 Mier Randall M Method of forming a permselective layer
US5200051A (en) * 1988-11-14 1993-04-06 I-Stat Corporation Wholly microfabricated biosensors and process for the manufacture and use thereof
JPH0765978B2 (ja) 1992-09-14 1995-07-19 日機装株式会社 微量成分測定方法及び微量成分測定装置
EP0752099A1 (de) * 1994-02-09 1997-01-08 Abbott Laboratories Vorrichtung mit durchflusszelle
US5814376A (en) * 1995-01-13 1998-09-29 Ohmicron Medical Diagnostics, Inc. Gravure coating systems and magnetic particles in electrochemical sensors
US6673533B1 (en) * 1995-03-10 2004-01-06 Meso Scale Technologies, Llc. Multi-array multi-specific electrochemiluminescence testing
EP0823054A1 (de) 1995-04-27 1998-02-11 Pharmacia Biotech AB Vorrichtung zur kontinuierlichen messung von physikalischen und chemischen parametern in einer strömung
US6413410B1 (en) * 1996-06-19 2002-07-02 Lifescan, Inc. Electrochemical cell
DE69809391T2 (de) * 1997-02-06 2003-07-10 Therasense, Inc. Kleinvolumiger sensor zur in-vitro bestimmung
DE19801344C2 (de) * 1998-01-16 2002-01-17 Trace Biotech Ag Durchfluss-Analysenzelle und zugehöriger Schichtsensor
US6878251B2 (en) * 1998-03-12 2005-04-12 Lifescan, Inc. Heated electrochemical cell
US6123820A (en) * 1998-06-05 2000-09-26 Grupo Ch-Werfen, S.A. Sensor cartridges
JP3874321B2 (ja) * 1998-06-11 2007-01-31 松下電器産業株式会社 バイオセンサ
JP3267936B2 (ja) * 1998-08-26 2002-03-25 松下電器産業株式会社 バイオセンサ
US6726818B2 (en) * 2000-07-21 2004-04-27 I-Sens, Inc. Biosensors with porous chromatographic membranes
JP2002174610A (ja) 2000-12-08 2002-06-21 Nec Corp バイオセンサ及びバイオセンサを用いた液体試料の測定方法
CN101158664A (zh) * 2002-07-31 2008-04-09 株式会社东芝 碱基序列检测装置及碱基序列自动解析装置
KR100482285B1 (ko) * 2002-10-30 2005-04-14 한국전자통신연구원 유로형 다중 전기 화학 시스템 및 그의 제조방법
CA3171720C (en) * 2002-12-26 2024-01-09 Meso Scale Technologies, Llc. Methods for conducting electrochemiluminescence measurements
CN1839313B (zh) * 2003-06-20 2011-12-14 霍夫曼-拉罗奇有限公司 涉及电化学生物传感器的设备和方法
US7118667B2 (en) * 2004-06-02 2006-10-10 Jin Po Lee Biosensors having improved sample application and uses thereof
WO2006113440A2 (en) * 2005-04-15 2006-10-26 Worcester Polytechnic Institute Multi-transduction mechanism based microfluidic analyte sensors
US20080100279A1 (en) * 2006-06-15 2008-05-01 University Of South Florida Nano-Based Device for Detection of Disease Biomarkers and Other Target Molecules
US7993512B2 (en) 2006-07-11 2011-08-09 Bayer Healthcare, Llc Electrochemical test sensor
JPWO2008044530A1 (ja) 2006-10-05 2010-02-12 パナソニック株式会社 多項目成分分析センサおよび多項目成分の測定方法
US11339430B2 (en) * 2007-07-10 2022-05-24 Life Technologies Corporation Methods and apparatus for measuring analytes using large scale FET arrays
CN101849180B (zh) 2007-09-24 2017-08-18 安晟信医疗科技控股公司 多区域分析物测试传感器
US20100301398A1 (en) * 2009-05-29 2010-12-02 Ion Torrent Systems Incorporated Methods and apparatus for measuring analytes
CN102317773B (zh) * 2009-01-23 2015-03-11 聚合物技术系统公司 具有一体生物传感器的诊断式多层干相测试条
CN104825171B (zh) 2009-02-26 2017-08-04 雅培糖尿病护理公司 改进的分析物传感器及其制造和使用方法
AU2011253076B2 (en) 2010-05-12 2014-05-01 Parker-Hannifin Corporation Sensor sleeve for health monitoring an article
TW201209405A (en) 2010-06-17 2012-03-01 Geneasys Pty Ltd Microfluidic device with flow-channel structure having active valve for capillary-driven fluidic propulsion without trapped air bubbles
US9215995B2 (en) 2010-06-23 2015-12-22 Medtronic Minimed, Inc. Sensor systems having multiple probes and electrode arrays
JP5856780B2 (ja) 2010-08-27 2016-02-10 シスメックス株式会社 検出物質の光電気化学的検出方法及び被検物質の光電気化学的検出方法
KR101363020B1 (ko) 2011-10-31 2014-02-26 주식회사 세라젬메디시스 다중 반응 바이오센서
JP6216585B2 (ja) * 2012-10-11 2017-10-18 株式会社堀場製作所 マルチイオンセンサ
US10545161B2 (en) * 2013-03-11 2020-01-28 Cue Health Inc. Systems and methods for detection and quantification of analytes
US9458488B2 (en) * 2013-03-15 2016-10-04 Nanomix, Inc. Point of care sensor systems
JP6475405B2 (ja) * 2013-05-07 2019-02-27 株式会社日立ハイテクノロジーズ 電解質濃度測定装置およびそれを用いた測定方法
EP2816345A1 (de) * 2013-06-19 2014-12-24 Roche Diagniostics GmbH Elektrolumineszenzverfahren zur Erkennung eines Analyts in einer Flüssigkeitsprobe und Analysesystem
EP3101413B1 (de) * 2014-01-31 2021-10-20 Hitachi High-Tech Corporation Ionenselektive elektrode vom durchflusstyp
WO2015151395A1 (ja) * 2014-03-31 2015-10-08 パナソニックIpマネジメント株式会社 電気化学測定デバイス
US10814322B2 (en) 2014-07-09 2020-10-27 Siemens Healthcare Diagnostics Inc. Low sample volume sensing device
EP3169992B1 (de) * 2014-07-17 2022-10-19 Siemens Healthcare Diagnostics Inc. Sensoranordnung
FR3025440A1 (fr) 2014-09-05 2016-03-11 Centre Nat Rech Scient Dispositif et procede d'analyse microfluidique
CN107003265B (zh) 2014-12-12 2021-08-24 松下知识产权经营株式会社 电化学测量装置
US20230408510A1 (en) * 2014-12-18 2023-12-21 Cardea Bio, Inc. Chemically-sensitive field effect transistors, systems, and methods for manufacturing and using the same
WO2016106320A2 (en) * 2014-12-22 2016-06-30 Siemens Healthcare Diagnostics Inc. Foldable opposing sensor array
JP6539918B2 (ja) * 2015-03-07 2019-07-10 国立大学法人名古屋大学 参照電極保持部材及び物質検出装置
DK3329265T3 (da) * 2015-07-30 2023-06-26 Siemens Healthcare Diagnostics Inc Sensoranordning
WO2017027477A1 (en) 2015-08-07 2017-02-16 Fraunhofer Usa, Inc. Apparatus and method for detecting trace metals with electrically conductive diamond electrodes
JP2017053808A (ja) 2015-09-11 2017-03-16 株式会社東芝 半導体分析チップ及び微粒子検査方法
WO2017120464A1 (en) * 2016-01-08 2017-07-13 Siemens Healthcare Diagnostics Inc. Heating element for sensor array
US20170010259A1 (en) * 2016-06-12 2017-01-12 Ghassem Amoabediny Multiplexed microfluidic proteomic platform
US9829456B1 (en) * 2016-07-26 2017-11-28 Roswell Biotechnologies, Inc. Method of making a multi-electrode structure usable in molecular sensing devices
US11198129B2 (en) * 2016-10-05 2021-12-14 Abbott Laboratories Devices and methods for sample analysis
US10876997B2 (en) * 2017-07-27 2020-12-29 Taiwan Semiconductor Manufacturing Co., Ltd. Bio-field effect transistor device
CN111316072B (zh) * 2017-11-17 2021-12-07 美国西门子医学诊断股份有限公司 传感器组件和使用所述传感器组件的方法
US10830724B2 (en) * 2017-12-22 2020-11-10 International Business Machines Corporation Micro-capacitance sensor array containing spaced apart first and second overlapping and parallel electrode plates for sensing analytes
EP4016068A1 (de) * 2020-12-21 2022-06-22 F. Hoffmann-La Roche AG Sensoranordnung
EP4016069A1 (de) * 2020-12-21 2022-06-22 F. Hoffmann-La Roche AG Sensorvorrichtung und verfahren zu ihrer verwendung

Also Published As

Publication number Publication date
CN111316072A (zh) 2020-06-19
CN111316072B (zh) 2021-12-07
EP3710790A4 (de) 2021-01-20
CA3082898C (en) 2023-03-14
IL274468A (en) 2020-06-30
CA3082898A1 (en) 2019-05-23
US20200278313A1 (en) 2020-09-03
WO2019099855A1 (en) 2019-05-23
MX2020005123A (es) 2020-11-06
US12072311B2 (en) 2024-08-27
JP2021503597A (ja) 2021-02-12
JP2022010070A (ja) 2022-01-14

Similar Documents

Publication Publication Date Title
US11850585B2 (en) Low sample volume sensing device
US20060141469A1 (en) Multi-layered electrochemical microfluidic sensor comprising reagent on porous layer
US20040040868A1 (en) Microfabricated sensor arrays for multi-component analysis in minute volumes
US20080241933A1 (en) Biological Saw Sensor
US11408882B2 (en) Sensor array
US9945804B2 (en) Sensor array
EP3400754B1 (de) Heizelement für sensoranordnung
CA3082898C (en) Sensor assembly and method of using same
JP5343258B2 (ja) 生体物質を測定するバイオセンサ
US20230271185A1 (en) Biosensor system for multiplexed detection of biomarkers

Legal Events

Date Code Title Description
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE

PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE

17P Request for examination filed

Effective date: 20200610

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

AX Request for extension of the european patent

Extension state: BA ME

A4 Supplementary search report drawn up and despatched

Effective date: 20201218

RIC1 Information provided on ipc code assigned before grant

Ipc: G01N 27/327 20060101ALI20201214BHEP

Ipc: G01N 33/49 20060101AFI20201214BHEP

Ipc: G01N 33/543 20060101ALI20201214BHEP

DAV Request for validation of the european patent (deleted)
DAX Request for extension of the european patent (deleted)
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

17Q First examination report despatched

Effective date: 20221219